Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.439920
Title: Cannabinoid modulation of glutamate uptake and release from adult rat hippocampal synaptosomes
Author: Nisha, Parihar
ISNI:       0000 0001 3447 5766
Awarding Body: University of Aberdeen
Current Institution: University of Aberdeen
Date of Award: 2007
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Abstract:
CB1 receptors are confined to the nervous system; their expression within the hippocampus is localised to the presynpatic terminals of a subset of cholecystokinin containing GABA-ergic neurones, where they inhibit GABA release. Hippocampal glutamate release is also inhibited by cannabinoids but at the site of action and receptor involved is still to be identified. Studies of K+-evoked release of [3H]D-Aspartate from rat hippocampal synaptosomes suggest anadamide may not just be acting on presynpatic cannabinoid receptors, but also directly on glutamate uptake transporters. The current study aims to characterise cannabinoid-modulation of excitatory amino acid (EAA) release and uptake from hippocampal glutamatergic nerve terminals. Glutamate release from synaptosomes was quantified using spectrofluorimetry and uptake was quantified with [3H]EAA’s. Both the cannabinoids, (WIN55,212-2 and anandamide) inhibited evoked glutamate release in the absence of calcium. Interestingly, WIN55,212-2-inhibition was blocked by SR141716A (CB1 antagonist), whereas the response to anandamide was not. The non-selective EAA transporter (EAAT) blocker T3MG, inhibited anandamide-attenuation of evoked release. Anandamide reduced basal glutamate levels, where again, neither SR141716A nor capsazepine altered the response to anandamide, indicating these effects are not mediated by either CB1 or TRPV1 receptors. The action of anandamide was neither mimicked by arachidonic acid, nor affected by PMSF, (FAAH, fatty acid amide hydrolase) inhibitor, suggesting anandamide metabolism to arachidonic acid by FAAH is not required. Anandamide also stimulated [3H]L-glutamic acid uptake; this was attenuated by the non-selective EAAT blocker, DL-TBOA. We suggest that the effects of anandamide are mediated by interaction of the endocannabinoid with glutamate receptors.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.439920  DOI: Not available
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